Detection of Deletions/Duplications in α-Globin Gene Cluster by Multiplex Ligation-Dependent Probe Amplification-Reference-Cited by-同舟云学术

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Detection of Deletions/Duplications in α-Globin Gene Cluster by Multiplex Ligation-Dependent Probe Amplification

Published:2012-07 Issue:7 Volume:16 Page:684-688
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Nezhat Naghmeh¹,Akbari Mohammad Taghi²³

Affiliation:

1. Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

2. Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

3. Tehran Medical Genetics Laboratory, Tehran, Iran.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2011.0251

Reference18 articles.

1. Quantitative polmerase chain reaction for the rapid prenatal diagnosis of homozygous α-thalassaemia (Hb Barts hydrops fetalis)

2. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

3. Molecular diagnosis of haemoglobin disorders

4. Can the product of the θ gene be a real globin?

5. Novel large deletions in the human α-globin gene cluster: Clarifying the HS-40 long-range regulatory role in the native chromosome environment

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of a novel 91.5 kb-deletion (αα) ^FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing;The Journal of Maternal-Fetal & Neonatal Medicine;2023-09-06

2. Diagnosis of the accurate genotype of HKαα carriers in patients with thalassemia using multiplex ligation-dependent probe amplification combined with nested polymerase chain reaction;Chinese Medical Journal;2020-04-21

3. Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing;Molecular Genetics and Genomics;2020-01-02

4. Invasive prenatal diagnosis of fetal thalassemia;Best Practice & Research Clinical Obstetrics & Gynaecology;2017-02

5. Detection of α-Thalassemia by Using Multiplex Ligation-Dependent Probe Amplification as an Additional Method for Rare Mutations in Southern Turkey;Indian Journal of Hematology and Blood Transfusion;2015-11-13

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